Liquid crystal benzene derivatives
Benzene derivatives useful as a component of liquid crystal compositions are provided which are expressed by the general formula ##STR1## wherein R represents a hydrogen atom or an alkyl group of 1 to 10 carbon atoms; R' represents a hydrogen atom, an alkyl group of 1 to 10 carbon atoms or an alkoxy group of 1 to 10 carbon atoms; and ##STR2## represents ##STR3## The derivatives exhibit small values of positive dielectric anisotropy; have broader liquid crystal temperature ranges; and in particular, have higher liquid crystalline-transparent points and yet have lower viscosities.
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This invention relates to novel liquid crystal substances which exhibit a liquid crystal phase within broad temperature ranges and have lower viscosities.
Liquid crystal display elements utilize optical anisotropy and dielectric anisotropy of liquid crystal substances, and are classified into various types such as TN type (twisted nematic type), DS type (dynamic scattering type), guest-host type, DAP type, etc. according to their display modes, and the properties of liquid crystal substances suitable to their respective uses are different. However, it is common to any liquid crystals that stabilities to moisture, air, heat, light, etc. are required, and it is also necessary that they exhibit a liquid crystal phase within as broad a temperature range as possible, around room temperature, and further, have an optimal value of dielectric anisotropy (.DELTA..epsilon.) varied depending on the kinds of display elements. At present, however, no single compound which alone satisfies such conditions is present, and it is the present status that a liquid crystal composition obtained by blending several kinds of liquid crystal compounds or non-liquid-crystal compounds is used. Recently, display elements actuating over from lower temperatures (about -20.degree. C.) up to higher temperatures (about 80.degree.-90.degree. C.) have been particularly needed; thus, liquid crystal compositions having superior actuation characteristics within a broader temperature range have been desired.
The object of the present invention is to provide novel liquid crystal compounds which are useful as a component of such liquid crystal compositions and particularly suitable to improvement in low temperature characteristics.
SUMMARY OF THE INVENTIONThe present invention is directed to benzene derivatives expressed by the general formula ##STR4## wherein R represents a hydrogen atom or an alkyl group of 1 to 10 carbon atoms; R' represents a hydrogen atom, an alkyl group of 1 to 10 carbon atoms or an alkoxy group of 1 to 10 carbon atoms; and ##STR5## represents ##STR6##
DETAILED DESCRIPTION OF THE INVENTIONThe compounds of the present invention exhibit small values of positive dielectric anisotropy; have broader liquid crystal temperature ranges; and in particular, have higher liquid crystalline-transparent points (N-I points or Sm-I points) and yet have lower viscosities. Among the compounds of the formula (I), those wherein the group ##STR7## of formula (I) is ##STR8## are particularly stable to heat, air, moisture, light, etc.; hence they are extremely useful for preparing liquid crystal compositions actuating within a broad temperature range over from lower temperatures up to higher ones.
Next, a process for preparing compounds of the present invention will be illustrated below.
Bromobenzene (in the case where R=H) or a 4-substituted-bromobenzene (in the case where R is other than H) is first reacted with metallic magnesium in tetrahydrofuran to give a 4-substituted-(or unsubstituted-)phenylmagnesium bromide (terms "or unsubstituted" will be omitted below), which is then reacted with 4-cyclohexylcyclohexanone (in the case where R=H) or a 4-(trans-4'-alkylcyclohexyl) cyclohexanone (in the case where R is other than H) (these cyclohexanones being obtained by oxidizing the corresponding cyclohexanols with anhydrous chromic acid), to give a 4-substituted-[1'-hydroxy-4'-(trans-4"-alkylcyclohexyl) cyclohexyl]benzene, which is then dehydrated in the presence of potassium hydrogen sulfate as catalyst, to give a 4-substituted-[4'-(trans-4"-alkylcyclohexyl)cyclohexen-1'-yl]benzene as one of the objective compounds. This compound is further reduced in ethanol as solvent in the presence of Raney nickel catalyst under the atmospheric pressure and at 30.degree. C. to give a 4-substituted-[4'-(trans-4"-alkylcyclohexyl)cyclohexyl]benzene. Since this compound is a mixture of trans-form with cis-form, it is recrystallized from ethanol to give an objective 4-substituted-[trans-4'-(trans-4"-alkylcyclohexyl) cyclohexyl]benzene. The above reactions can be illustrated by chemical equations as follows: ##STR9## (In the above equations, R and R' are the same groups as defined above.)
The process for preparing compounds of the present invention and the use examples thereof will be further described in detail by way of Examples.
EXAMPLE 1 Preparation of 4-methoxy-[4'-(trans-4"-propylcyclohexyl)cyclohexen-1'-yl]benzeneA magnesium slice (1.2 g, 0.049 mol) was placed in a three-neck flask, and 30 ml of a solution of 4-bromoanisole (9.2 g, 0.049 mol) dissolved in tetrahydrofuran was slowly dropwise added with stirring in nitrogen gas current while the reaction temperature was maintained at 30.degree.-35.degree. C. As a result of the reaction, magnesium dissolved in 3 hours to form a uniform solution containing 4-methoxyphenylmagnesium bromide, to which 50 ml of a solution of 4-(trans-4'-propylcyclohexyl)cyclohexanone (10.9 g, 0.049 mol) dissolved in tetrahydrofuran was dropwise added as rapidly as possible while the reaction temperature was maintained at 5.degree.-10.degree. C. After the dropwise addition, the mixture was heated up to 35.degree. C. and agitated for 30 minutes, followed by adding 50 ml of 3 N hydrochloric acid. The reaction liquid was then taken into a separating funnel and subjected to extraction three times with toluene, followed by washing combined toluene layers with water till it became neutral and then distilling off toluene under reduced pressure to give as residue, 4-methoxy-[1'-hydroxy-4'-(trans-4"-propylcyclohexyl)cyclohexyl]benzene.
Potassium hydrogen sulfate (6 g) was added to it and the mixture was subjected to dehydration in nitrogen gas current at 160.degree. C. for 2 hours. After cooling, toluene (200 ml) was added and potassium hydrogen sulfate was filtered off, followed by washing the resulting toluene layer with water till the washing water became neutral. Toluene was then distilled off under reduced pressure to give an oily substance as residue which was recrystallized from ethanol to give objective 4-methoxy-[4'-(trans-4"-propylcyclohexyl)cyclohexene-1'-yl]benzene. This compound had a crystalline-smectic (C-Sm)point of 95.2.degree. C., a smectic-nematic (Sm-N) point of 139.2.degree. C. and a nematic-transparent (N-I)point of 207.4.degree. C. Yield: 7.0 g (46%). The fact that this product was an objective compound was confirmed by NMR spectra, IR absorption spectra and elementary analysis.
EXAMPLES 2-61Example 1 was repeated except that the carbon numbers of R and R' in the above formula (I.sub.a) were varied. The yields (g and %) and physical properties of the resulting compounds are shown in Table 1 together with those in Example 1.
TABLE 1
__________________________________________________________________________
##STR10##
Amount Phase transition
of raw points (.degree.C.)
material C-Sm N-I
4-substi- point point
tuted or or
Exam- hexanone
Yield C-I Sm-N
Sm-I
ple R R' used (g)
(g)
(%)
point point
point
__________________________________________________________________________
1 C.sub.3 H.sub.7
CH.sub.3 O
8.7 7.0
46 93.2 139.2
207.4
2 C.sub.3 H.sub.7
C.sub.3 H.sub.7 O
8.7 8.1
49 87.4 187.9
200.5
3 C.sub.3 H.sub.7
C.sub.7 H.sub.15 O
9.6 8.0
41 70.1 -- 193.6
4 C.sub.4 H.sub.9
C.sub.2 H.sub.5 O
9.2 5.1
31 81.8 182.6
202.2
5 C.sub.4 H.sub.9
C.sub.6 H.sub.13 O
9.2 5.0
26 72.6 -- 199.2
6 C.sub.5 H.sub. 11
C.sub.3 H.sub.7 O
9.8 5.2
29 81.0 -- 196.8
7 C.sub.6 H.sub.13
CH.sub.3 O
13.0 5.5
30 66.0 133.1
180.0
8 C.sub.6 H.sub.13
CH.sub.3
10.3 3.0
18 66.1 144.1
170.2
9 C.sub.7 H.sub.15
C.sub.3 H.sub.7 O
10.9 15.4
79 79.3 -- 195.9
10 C.sub.7 H.sub.15
C.sub.7 H.sub.15 O
1.0 0.9
55 79.6 -- 192.0
11 H H 7.7 5.5
43 97.7 -- --
.about.98.4
12 C.sub.3 H.sub.7
H 26.2 19.4
48 68.6 77.1
105.5
13 C.sub.4 H.sub.9
H 9.2 4.7
32 75.8 89.0
104.8
14 C.sub.5 H.sub.11
H 29.5 19.5
42 69.8 83.9
111.8
15 H CH.sub.3 O
21.3 16 50 115.0 -- --
.about.116.0
16 H C.sub.2 H.sub.5 O
21.3 20 60 109.8 -- 119.1
17 H C.sub.3 H.sub.7 O
21.3 10 29 100.3 -- 118.0
18 H C.sub.4 H.sub.9 O
21.3 19 52 73.5 -- 112.1
19 H C.sub.5 H.sub.11 O
21.3 22 58 73.5 -- 108.6
20 C.sub.2 H.sub.5
CH.sub.3
8.3 4.2
40 74.8 130.2
151.5
21 C.sub.2 H.sub.5
C.sub.2 H.sub.5
8.3 1.6
15 room -- 155.9
temp.
or lower
22 C.sub.2 H.sub.5
C.sub.3 H.sub.7
8.3 1.8
15 room -- 156.2
temp.
or lower
23 C.sub.2 H.sub.5
C.sub.5 H.sub.11
8.3 1.5
8 room -- 153.7
temp.
or lower
24 C.sub.2 H.sub.5
C.sub.6 H.sub.13
8.3 2.2
15 room -- 150.6
temp.
or lower
25 C.sub.3 H.sub.7
CH.sub.3
8.9 3.0
25 80.5 133.3
180.8
26 C.sub.3 H.sub.7
C.sub.3 H.sub.7
8.9 6.0
45 57.0 -- 163.7
27 C.sub.3 H.sub.7
C.sub.4 H.sub.9
8.9 3.0
22 room -- 176.3
temp.
or lower
28 C.sub.3 H.sub.7
C.sub.5 H.sub.11
8.9 2.7
19 room -- 175.0
temp.
or lower
29 C.sub.3 H.sub.7
C.sub.6 H.sub.13
8.9 1.1
8 room -- 173.4
temp.
or lower
30 C.sub.3 H.sub.7
C.sub.2 H.sub.5 O
13.3 9.5
29 80.0 170.0
208.5
31 C.sub.3 H.sub.7
C.sub.4 H.sub.9 O
8.7 1.6
12 60.2 -- 195.6
32 C.sub.3 H.sub.7
C.sub.5 H.sub.11 O
6.4 2.2
21 75.8 181.0
197.2
33 C.sub.3 H.sub.7
C.sub.6 H.sub.13 O
10.1 4.4
25 71.3 -- 192.7
34 C.sub.5 H.sub.11
CH.sub.3
10.0 4.4
34 70.4 141.8
174.4
35 C.sub.5 H.sub.11
C.sub.3 H.sub.7
10.0 6.7
48 54.6 172.3
175.6
36 C.sub.5 H.sub.11
C.sub.4 H.sub.9
10.0 1.0
7 room -- 182.0
temp.
or lower
37 C.sub.5 H.sub.11
C.sub.5 H.sub.11
10.0 6.1
40 room -- 181.0
temp.
or lower
38 C.sub.5 H.sub.11
C.sub.6 H.sub.13
10.0 7.3
45 room -- 182.0
temp.
or lower
39 C.sub.5 H.sub.11
CH.sub.3 O
9.8 2.5
15 83.0 148.8
199.6
40 C.sub.5 H.sub.11
C.sub.2 H.sub.5 O
7.3 3.0
29 84.9 189.4
204.0
41 C.sub.5 H.sub.11
C.sub.4 H.sub.9 O
9.8 5.6
38 65.5 -- 208.3
42 C.sub.5 H.sub.11
C.sub.5 H.sub.11 O
7.3 1.8
12 75.8 -- 206.0
43 C.sub.5 H.sub.11
C.sub.6 H.sub.13 O
7.4 7.2
62 73.6 -- 203.3
44 C.sub.5 H.sub.11
C.sub.7 H.sub.15 O
11.4 7.4
38 83.7 -- 196.8
45 C.sub.7 H.sub.15
CH.sub.3 O
7.5 8.0
60 81.1 147.3
182.0
46 C.sub.2 H.sub.5
C.sub.4 H.sub.9
8.3 3.5
27 room -- 150.7
temp.
or lower
47 C.sub.2 H.sub.5
C.sub.7 H.sub.15
8.3 1.0
7 room -- 139.6
temp.
or lower
48 C.sub.2 H.sub.5
C.sub.8 H.sub.17
8.3 4.4
30 room -- 148.4
temp.
or lower
49 C.sub.3 H.sub.7
C.sub.7 H.sub.15
8.9 2.8
19 room -- 165.9
temp.
or lower
50 C.sub.4 H.sub.9
CH.sub.3
9.5 6.3
51 76.7 130.1
170.4
51 C.sub.4 H.sub.9
C.sub.2 H.sub.5
9.5 4.5
35 37.3 -- 163.9
52 C.sub.4 H.sub.9
C.sub.3 H.sub.7
9.5 1.6
12 room -- 181.6
temp.
or lower
53 C.sub.4 H.sub.9
C.sub.5 H.sub.11
9.5 2.6
18 room -- 181.8
temp.
or lower
54 C.sub.5 H.sub.11
C.sub.7 H.sub.15
10.0 2.0
12 room -- 174.5
temp.
or lower
55 C.sub.7 H.sub.15
CH.sub.3
11.1 2.5
18 67.4 147.9
174.6
56 C.sub.7 H.sub.15
C.sub.2 H.sub.5
11.1 8.2
56 42.6 163.3
165.5
57 C.sub.7 H.sub.15
C.sub.3 H.sub.7
11.1 9.0
59 40.8 -- 171.8
58 C.sub.7 H.sub.15
C.sub.4 H.sub.9
11.1 11.6
74 room -- 179.3
temp.
or lower
59 C.sub.7 H.sub.15
C.sub.5 H.sub.11
11.1 10.0
61 room -- 182.0
temp.
or lower
60 C.sub.7 H.sub.15
C.sub.6 H.sub.13
11.1 9.0
53 room -- 179.8
temp.
or lower
61 C.sub.7 H.sub.15
C.sub.7 H.sub.15
11.1 5.1
29 49.9 -- 179.4
__________________________________________________________________________
EXAMPLE 62
Preparation of 4-methoxy-[trans-4'-(trans-4"-propylcyclohexyl)cyclohexyl]benzene
4-Methoxy-[4'-(trans-4"-propylcyclohexyl)cyclohexen-1'-yl]benzene (7.0 g) prepared in Example 1 was dissolved in ethanol (120 ml) and Raney nickel catalyst (1.0 g) was added, followed by catalytic reduction at 50.degree. C. under the atmospheric pressure (the quantity of hydrogen absorbed: 500 ml). After filtering off the catalyst, the solution was subjected to recrystallization as it was. Since the resulting material was a mixture of cis-form with trans-form, it was further repeatedly recrystallized from ethanol to isolate the trans-form. This compound was 4-methoxy-[trans-4'-(trans-4"-propylcyclohexyl)cyclohexyl]benzene, and had a crystalline-smectic (C-Sm) point of 79.2.degree. C., a smectic-nematic (Sm-N) point of 128.4.degree. C. and a nematic-transparent (N-I) point of 211.5.degree. C. Yield: 2.8 g (40%). The fact that this product was an objective compound was confirmed by NMR spectra and elementary analysis.
EXAMPLES 63-108Example 62 was repeated except that the carbon numbers of the alkyl group and the alkoxy group were varied. The yields and physical properties of the resulting compounds are shown in Table 2 together with those in Example 62.
TABLE 2
______________________________________
##STR11##
Phase transition points
(.degree.C.)
Ex- C-Sm point N-I point
am- Yield or Sm-N or Sm-I
ple R R' (%) C-I point
point point
______________________________________
62 C.sub.3 H.sub.7
CH.sub.3 O
40 79.2 128.4 211.5
63 C.sub.3 H.sub.7
C.sub.3 H.sub.7 O
24 81.6 179.5 201.4
64 C.sub.3 H.sub.7
C.sub.7 H.sub.15 O
40 72.1 172.0 178.0
65 C.sub.4 H.sub.9
C.sub.2 H.sub.5 O
30 84.7 172.5 211.5
66 C.sub.4 H.sub.9
C.sub.6 H.sub.13 O
19 70.0 -- 186.3
67 C.sub.5 H.sub.11
C.sub.3 H.sub.7 O
38 56.3 195.1 201.8
68 C.sub.6 H.sub.13
CH.sub.3 O
22 70.5 154.5 196.5
69 C.sub.6 H.sub.13
CH.sub.3 12 135.8 142.5 167.8
70 C.sub.7 H.sub.15
C.sub.3 H.sub.7 O
32 62.7 -- 194.6
71 C.sub.7 H.sub.15
C.sub.7 H.sub.15 O
20 58.1 -- 188.0
72 C.sub.3 H.sub.7
H 23 75.9 91.8 100.4
73 C.sub.4 H.sub.9
H 35 70.1 -- 109.2
74 C.sub.5 H.sub.11
H 15 61.6 107.9 111.8
75 H CH.sub.3 O
31 92.8 -- --
76 H C.sub.2 H.sub.5 O
25 87.0 -- 98.7
77 H C.sub.3 H.sub.7 O
30 90.4 -- 113.0
78 H C.sub.4 H.sub.9 O
20 85.3 -- 101.0
79 H C.sub.5 H.sub.11 O
20 62.4 -- 87.2
80 C.sub.3 H.sub.7
CH.sub.3 20 64.6 109.7 179.8
81 C.sub.3 H.sub.7
C.sub.2 H.sub.5
13 31.0 161.3 162.7
82 C.sub.3 H.sub.7
C.sub.3 H.sub.7
20 room temp.
-- 177.5
or lower
83 C.sub.3 H.sub.7
C.sub.2 H.sub.5 O
5 84.6 149.1 210.1
84 C.sub.3 H.sub.7
C.sub.4 H.sub.9 O
38 65.3 179.1 190.9
85 C.sub.3 H.sub.7
C.sub.5 H.sub.11 O
21 60.8 175.8 185.6
86 C.sub.3 H.sub.7
C.sub.6 H.sub.13 O
27 77.0 175.3 185.3
87 C.sub.4 H.sub.9
CH.sub.3 33 58.0 135.2 173.9
88 C.sub.5 H.sub.11
CH.sub.3 39 55.8 138.0 178.6
89 C.sub.5 H.sub.11
C.sub.2 H.sub.5
26 37.8 -- 173.2
90 C.sub.5 H.sub.11
C.sub.3 H.sub.7
16 48.6 -- 181.0
91 C.sub.5 H.sub.11
C.sub.4 H.sub.9
18 room temp.
-- 190.6
or lower
92 C.sub.5 H.sub.11
CH.sub.3 O
30 66.3 150.1 207.7
93 C.sub.5 H.sub.11
C.sub.2 H.sub.5 O
27 81.8 176.3 215.2
94 C.sub.5 H.sub.11
C.sub.4 H.sub.9 O
7 63.2 199.2 200.6
95 C.sub.5 H.sub.11
C.sub.5 H.sub.11 O
16 61.4 -- 196.7
96 C.sub.5 H.sub.11
C.sub.6 H.sub.13 O
10 58.1 -- 192.5
97 C.sub.7 H.sub.15
CH.sub.3 O
22 68.8 153.0 194.7
98 C.sub.2 H.sub.5
CH.sub.3 10 62.8 103.7 142.3
99 C.sub.2 H.sub.5
C.sub.2 H.sub.5
6 55.1 -- 151.9
100 C.sub.2 H.sub.5
C.sub.3 H.sub.7
9 room temp.
-- 160.8
or lower
101 C.sub.2 H.sub.5
C.sub.4 H.sub.9
23 room temp.
-- 158.6
or lower
102 C.sub.2 H.sub.5
C.sub.5 H.sub.11
17 room temp.
-- 151.0
or lower
103 C.sub.2 H.sub.5
C.sub.6 H.sub.13
21 room temp.
-- 148.6
or lower
104 C.sub.3 H.sub.7
C.sub.4 H.sub.9
31 room temp.
-- 189.6
or lower
105 C.sub.3 H.sub.7
C.sub.5 H.sub.11
19 room temp.
-- 172.2
or lower
106 C.sub.3 H.sub.7
C.sub.6 H.sub.13
10 room temp.
-- 171.0
or lower
107 C.sub.5 H.sub.11
C.sub.5 H.sub.11
11 room temp.
-- 189.8
or lower
108 C.sub.5 H.sub.11
C.sub.6 H.sub.13
7 room temp.
-- 185.9
or lower
______________________________________
Next, use examples will be described. Parts referred to herein are by weight.
EXAMPLE 109 (USE EXAMPLE 1)A liquid crystal composition (A) consisting of
trans-4-propyl-(4'-cyanophenyl)cyclohexane (28%),
trans-4-pentyl-(4'-cyanophenyl)cyclohexane (43%), and
trans-4-heptyl-(4'-cyanophenyl)cyclohexane (29%),
has a nematic temperature range of -3.degree.-+52.degree. C., a dielectric anisotropy value .DELTA..epsilon. of +10.5, a threshold voltage of 1.53 V and a saturation voltage of 2.12 V. Also it has a viscosity of 23 cp at 20.degree. C.
To this liquid crystal composition A (80 parts) were added 4-methoxy-[4'-(trans-4"-propylcyclohexyl)cyclohexen-1'-yl]benzene (10 parts) prepared in Example 1 and 4-ethoxy-[4'-(trans-4"-butylcyclohexyl)cyclohexen-1'-yl]benzene (10 parts) prepared in Example 4 to give a liquid crystal mixture. This mixture had as greatly extended a nematic temperature range as -10.degree.-+81.0.degree. C. Its .DELTA..epsilon. was reduced down to 8.8 and its threshold voltage and saturation voltage were elevated up to 1.63 V and 2.28 V, respectively and nevertheless its viscosity (23 cp) was unchanged.
EXAMPLE 110 (USE EXAMPLE 2)To the above liquid crystal composition (A) (90 parts) was added 4'-(trans-4"-pentylcyclohexyl)cyclohexen-1'-yl-benzene (10 parts) prepared in Example 14 to give a liquid crystal mixture. This mixture had as extended a nematic temperature range as -5.degree.-+58.degree. C. Its .DELTA..epsilon., threshold voltage and saturation voltage were elevated up to +9.0, 1.60 V and 2.30 V, respectively, but its viscosity (23 cp) was unchanged.
EXAMPLE 111 (USE EXAMPLE 3)To the liquid crystal composition (A) (80 parts) were added 4-methoxy-[trans-4'-(trans-4"-propylcyclohexyl)cyclohexyl]benzene (10 parts) prepared in Example 62 and 4-methoxy-[trans-4'-(trans-4"-hexylcyclohexyl)cyclohexyl]benzene (10 parts) prepared in Example 68 to give a liquid crystal mixture. This mixture had as extended a nematic temperature range as -10.degree.-+78.degree. C. Its .DELTA..epsilon. was reduced down to +8.8 and its threshold voltage and saturation voltage were elevated up to 1.63 V and 2.28 V, respectively, but its viscosity (23 cp) was unchanged. Thus it is seen that the compounds of the present invention are effective for lower temperature actuation.
EXAMPLE 112 (USE EXAMPLE 4)To the liquid crystal composition (A) (60 parts) were added [trans-4'-(trans-4"-propylcyclohexyl)cyclohexyl]benzene (20 parts) prepared in Example 72 and [trans-4'-(trans-4"-pentylcyclohexyl)cyclohexyl]benzene (20 parts) prepared in Example 74 to give a liquid crystal mixture. This mixture had as extended a nematic temperature range as -5.degree.-+73.degree. C. Its .DELTA..epsilon. was reduced down to +7.2 and its threshold voltage and saturation voltage were somewhat elevated up to 1.75 V and 2.30 V, respectively, but its viscosity (23 cp) was unchanged. Thus, by adding the compounds of the present invention, it was possible to extend the nematic temperature range with slight increases in the threshold voltage and saturation voltage in spite of reduction in the dielectric anisotropy value.
EXAMPLE 113 (USE EXAMPLE 5)A liquid crystal composition consisting of
4-pentyl-4'-cyanobiphenyl (45%),
4-heptyl-4'-cyanobiphenyl (29%),
4-octyloxy-4'-cyanobiphenyl (15%) and
4-pentyl-4'-cyanoterphenyl (11%),
had a N-I point of 63.3.degree. C. and a viscosity of 48 cp at 20.degree. C.
To this composition (95 parts) was added 1-(trans-4'-cyclohexylcyclohexyl)-4-propoxybenzene (5 parts) prepared in Example 77 to give a liquid crystal mixture having a N-I point of 61.8.degree. C. and a viscosity of 47.5 cp at 20.degree. C.
EXAMPLE 114 (USE EXAMPLE 6)A composition consisting of
4-pentyl-4'-cyanobiphenyl (51%),
4-heptyl-4'-cyanobiphenyl (32%) and
4-octyloxy-4'-cyanobiphenyl (17%),
had a N-I point of 44.3.degree. C. and a viscosity of 40 cp at 20.degree. C.
To this composition (90 parts) was added 1-(trans-4'-cyclohexylcyclohexyl)-4-methoxybenzene (10 parts) prepared in Example 75 to give a liquid crystal mixture having a N-I point of 44.1.degree. C. and a viscosity of 39 cp at 20.degree. C.
Claims
1. A benzene derivative expressed by the formula ##STR12## wherein R represents a hydrogen atom or an alkyl group of 1 to 10 carbon atoms; R' represents a hydrogen atom, an alkyl group of 1 to 10 carbon atoms or an alkoxy group of 1 to 10 carbon atoms; ##STR13## represents ##STR14## and wherein either one of R or R' must be an alkyl or alkoxy group.
2. A 4-Substituted or unsubstituted-[trans-4'-(trans-4"-alkylcyclohexyl)cyclohexyl]benzene expressed by the formula ##STR15## wherein R represents a hydrogen atom or an alkyl group of 1 to 10 carbon atoms; R' represents a hydrogen atom, an alkyl group of 1 to 10 carbon atoms or an alkoxy group of 1 to 10 carbon atoms, and wherein either one of R or R' must be an alkyl or alkoxy group.
3. A 4-Substituted or unsubstituted-[4'-(trans-4"-alkylcyclohexyl)cyclohexen-1'-yl]benzene expressed by the formula ##STR16## wherein R represents a hydrogen atom or an alkyl group of 1 to 10 carbon atoms; R' represents a hydrogen atom, an alkyl group of 1 to 10 carbon atoms or an alkoxy group of 1 to 10 carbon atoms, and wherein either one of R or R' must be an alkyl or alkoxy group.
4. A liquid crystal composition comprising a mixture of compounds at least one of which is a compound as claimed in claim 1.
5. In a liquid crystal display cell using a liquid crystal composition, the improvement which comprises a mixture of compounds at least one of which is a compound as claimed in claim 1.
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Type: Grant
Filed: Mar 16, 1982
Date of Patent: Dec 27, 1983
Assignee: Chisso Corporation (Osaka)
Inventors: Shigeru Sugimori (Kanagawaken), Tetsuhiko Kojima (Kanagawaken), Masakazu Tsuji (Kanagawaken)
Primary Examiner: Teddy S. Gron
Law Firm: Wenderoth, Lind & Ponack
Application Number: 6/358,794
International Classification: G02F 113; C09K 334; C07C 4321; C07C 1328;
